Department of Chemistry, University of North Bengal, Darjeeling 734 013, India.
J Colloid Interface Sci. 2013 Dec 1;411:152-61. doi: 10.1016/j.jcis.2013.08.034. Epub 2013 Sep 3.
In this contribution, we report on a systematic investigation of phase behavior and solubilization of water in water-in-heptane or decane aggregates stabilized by mixtures of polyoxyethylene (20) cetyl ether (Brij-58) and cetyltrimethylammonium bromide (CTAB) surfactants with varying compositions in conjugation with 1-pentanol (Pn) at fixed surfactant(s)/Pn ratio and temperature. Synergism in water solubilization was evidenced by the addition of CTAB to Brij-58 stabilized system in close proximity of equimolar composition in both oils. An attempt has been made to correlate composition dependent water solubilization and volume induced conductivity studies to provide insight into the solubilization mechanism of these mixed systems. Conductivity studies reveal the ascending curve in water solubilization capacity-(Brij-58:CTAB, w/w) profile as the interdroplet interaction branch indicating percolation of conductance and the descending curve is a curvature branch due to the rigidity of the interface in these systems. The microstructure of these systems as a function of surfactant composition has been determined by dynamic light scattering (DLS) and Fourier transform infrared spectroscopy (FTIR) measurements. FTIR study reveals increase and decrease in relative population of bound and bulk-like water, respectively, with increase in Brij-58:CTAB (w/w). DLS measurements showed that the droplet hydrodynamic diameter (Dh) decreases significantly with the increase in Brij-58:CTAB (w/w). Further, the interfacial composition and energetic parameters for the transfer of Pn from bulk oil to the interface were evaluated by the dilution method. Formation of temperature-insensitive microemulsions and temperature invariant droplet sizes are evidenced in the vicinity of the equimolar composition. The results are interpreted in terms of a proposed mechanism.
在本研究中,我们系统地研究了由聚氧乙烯(20)鲸蜡醚(Brij-58)和十六烷基三甲基溴化铵(CTAB)表面活性剂混合物稳定的庚烷或癸烷水包油乳液的相行为和水增溶作用,这些表面活性剂混合物的组成随正戊醇(Pn)的变化而变化,固定表面活性剂(s)/Pn 比和温度。在两种油中,当接近等摩尔组成时,CTAB 对 Brij-58 稳定体系的添加证明了水增溶的协同作用。尝试将依赖于组成的水增溶和体积诱导电导率研究相关联,以深入了解这些混合体系的增溶机制。电导率研究表明,在水增溶能力-(Brij-58:CTAB,w/w) 分布中,上升曲线作为指示电导率渗透的液滴间相互作用分支,下降曲线是由于这些体系界面刚性的曲率分支。通过动态光散射(DLS)和傅里叶变换红外光谱(FTIR)测量确定了这些体系的微结构作为表面活性剂组成的函数。FTIR 研究表明,随着 Brij-58:CTAB(w/w)的增加,结合水和体相水的相对比例分别增加和减少。DLS 测量表明,随着 Brij-58:CTAB(w/w)的增加,液滴水动力直径(Dh)显著减小。此外,通过稀释法评估了 Pn 从体油向界面转移的界面组成和能量参数。在等摩尔组成附近,证明了形成温度不敏感的微乳液和温度不变的液滴尺寸。结果根据提出的机制进行解释。